Electrodialysis methods for purification and recovery of gluconic acid derivatives

ABSTRACT

A process for purifying and concentrating a gluconic acid derivative, such as 2-keto-L-gulonic acid, comprising introducing a non-viable and/or acidified fermentation medium or an in-vitro reactor medium comprising at least the gluconic acid derivative and/or salt thereof to electrodialysis thereby purifying and concentrating the gluconic acid derivative.

CROSS REFERENCE TO RELATED APPLICATION

This application is a divisional of Ser. No. 08/318,348 filed May 25,1999 now U.S. Pat. No. 6,187,570 claims the benefit of U.S. ProvisionalApplication Ser. No. 60/086,792 filed May 26, 1998.

TECHNICAL FIELD

This invention relates generally to electrodialysis methods forseparation and purification of preferred end products and in particularto electrodialysis methods for the purification and recovery of gluconicacid derivatives, such as 2-keto-L-gulonic acid from solutions removedfrom fermentation reactors and in-vitro reactors.

BACKGROUND OF THE INVENTION

A gluconic acid derivative, namely 2-keto-L-gulonic acid (hereinafterKLG), is a key intermediate in the production of valuable compoundsincluding ascorbic acid (Vitamin C). However, to obtain high yieldsduring the conversion of KLG to ascorbic acid, the KLG must be highlypurified with a limited amount of impurities.

A convenient method for producing KLG is through a fermentation process.However, since most fermentation broths are maintained at neutral ornear neutral pHs by the addition of basic substances, salts of KLGrather than KLG are produced. Furthermore, the fermentation broth alsocontains cells, neutrals and other undesirable materials. Theseadditional components may interfere with the downstream chemistry usedto convert KLG to ascorbic acid, therefore, the KLG must be isolatedfrom the broth. Thus understood, any fermentation process for KLG mustbe integrated with an efficient recovery and purification process.

U.S. Pat. No. 5,747,306 discloses a method of separation usingelectrodialysis. The viable fermentation broth is maintained at a nearneutral or basic pH of between 5 and 9 by the addition of basicsubstances such as sodium hydroxide, potassium hydroxide or ammonia. Thebroth is then passed through an electrodialysis tank which containsrepeating cation and anion exchange membranes wherein the salts of KLGare removed from the broth. The viable fermentation broth containingneutrals, such as nutrients to insure survival of the microorganisms, isthen recirculated into the fermentation system for reuse. However, theelectrodialysis process produces a stream of purified KLG salt whichgives lower yields during the conversion to ascorbic acid.

Additionally, the prior art process of converting organic sugars to thesalt of KLG by using live and metabolically active microorganisms iscomplicated and demands constant vigilance to maintain a viable andactive fermentation broth for the growth and/or metabolism of themicroorganisms to ensure acceptable conversion of the substrate to theKLG salt.

To overcome the problems related with a high concentration of KLG saltsduring recovery of KLG from a fermentation medium, U.S. Pat. No.4,990,441 discloses a method of acidifying the fermentation medium withsulfuric acid thereby precipitating the salt cation with the sulfateanion and protonating the KLG anion. However, it should be noted, thatthe medium containing salts of KLG also contains inorganic impuritiessuch as phosphate and chloride anions which will also be converted totheir corresponding acids with the addition of sulfuric acid. As aresult, these inorganic acids can be concentrated during the KLGrecovery processes, such as evaporative crystallization or direct dryingand can cause acid catalyzed degradation of KLG. To rectify this problemthe prior art contacts the medium containing the KLG and otherimpurities with a cation and anion exchange resin to remove any ionizedimpurities. But, neutral organics present in the fermentation brothwhich include simple and complex sugars may be unionized at the solutionpH and thus not removed by passing the medium through cation and anionexchange resins. As such, the recovery of purified KLG is limited by thepresence of these neutrals in the medium. The neutral sugars areconcentrated during evaporative crystallization of KLG which causesincreased viscosity of the mother liquor. As a result, multiple passcrystallization becomes difficult and KLG recovery is limited. Also, theneutrals interfere with direct drying which is a preferred method ofrecovery because of higher KLG yield with lower capital costs.

Accordingly, methods are needed for the concentration and purificationof gluconic acid derivatives, such as KLG, which provide a higherrecovery yield of KLG without the salts thereof, without contaminationby inorganic impurities and neutral organics and/or without the need tomaintain a fermentation medium for the growth and/or metabolism of aliving and active culture of microorganisms.

SUMMARY OF THE INVENTION

For purposes of this invention, the terms and expressions below,appearing in the specification and claims, are intended to have thefollowing meanings:

“Gluconic acid derivative” is defined as an organic acid derived fromgluconic acid including, but not limited to, 2,4, keto-D-gluconic acid,2,5, diketo-D-gluconic acid, idonic acid, 2-keto-L-gulonic acid (KLG),vanillic acid and ascorbic acid.

“Fermentation reactor” is defined as a classical fermentation reactorwherein live and viable microorganisms or cells such as bacteria areused for metabolizing carbohydrates.

“Fermentation medium ” is a medium or broth derived from a classicalfermentation reactor.

“In vitro reactor” is a reactor wherein enzymes being substantially freeof non-living, non-viable and non-metabolizing cell structures, enzymesattached to non-living, non-viable and non-metabolizing cell structuresor enzymes immobilized on a substrate have the ability to chemicallyoxidize and/or chemically reduce substrates or intermediates on the pathto synthesizing gluconic acid derivatives.

“In vitro reactor medium” is a medium or solution derived from an invitro reactor comprising at least a salt of a gluconic acid derivativeand a coenzyme.

“Coenzyme” is an organic molecule required for the catalytic functioningof an enzyme, such as nicotinamide, adenine dinucleotide, nicotinamideadenine dinucleotide phosphate and mixtures thereof

“Neutrals” are defined as sugars and/or compounds that are substantiallyunionized at the solution's pH.

“Non-viable fermentation medium” means the conditions in thefermentation broth or medium, such as pH, are such that themicroorganisms used in the fermentation process are incapable ofsurvival therein and the medium or broth may not be recirculated backinto the fermentation tank for reuse without pretreatment.

“Non-living medium” means a medium removed from a fermentation reactoror in-vitro reactor such as a non-viable fermentation medium or in-vitroreactor medium wherein no living cells or living microorganisms capableof growth and/or metabolic activity for producing gluconic acidderivatives and/or salts thereof are present.

It is the principal object of this invention to provide novelelectrodialysis methods for the concentration and purification ofgluconic acid derivatives from an acidified and/or non-viablefermentation medium or an in-vitro reactor medium.

It is another object of the present invention to provide electrodialysispurification methods that result in higher recovery of KLG withsubsequent higher yields of ascorbic acid thereby realizing lowercapital and operating costs in the production of ascorbic acid.

It is a further object of the present invention to provide anelectrodialysis purification method that results in a recovered productthat will not be subject to acid catalyzed degradation and can makemultiple passes through an evaporation crystallization recovery processbecause of reduced viscosity of the mother liquid.

It is still further an object of the present invention to provide anelectrodialysis purification method that concentrates the end product,such as KLG, to such a high level of purity that direct drying of KLGcan be employed giving near quantitative recovery of same.

It is another object of the present invention to provide anelectrodialysis purification method that allows the recovery ofexpensive coenzymes and/or enzymes used in an in vitro reactor systemfor chemically synthesizing the salts of a gluconic acid derivative suchas KLG.

All of the above objects may be accomplished by an electrodialysispurification method comprising the following steps of:

a) providing a non-living medium, such as an acidified and/or non-viablefermentation medium or an in vitro reactor medium comprising at least agluconic acid derivative and/or salt thereof; and

b) removing the gluconic acid derivative from the non-living medium byelectrodialysis thereby providing a concentrated solution comprising atleast the gluconic acid derivative.

It is an additional object of the present invention to provide processesfor preparing purified and concentrated gluconic acid derivativescomprising the following steps of:

a) providing an acidified and/or non-viable fermentation mediumcomprising at least a gluconic acid derivative, an inorganic impurityand a neutral, wherein the gluconic acid derivative is substantiallyprotonated;

b) removing the gluconic acid derivative and inorganic impurity from theacidified and/or non-viable fermentation medium by electrodialysisthereby providing a concentrated acidified aqueous solution comprisingat least the gluconic acid derivative and inorganic impurity;

c) separating the inorganic impurity from the concentrated acidifiedaqueous solution thereby providing a purified and concentrated aqueoussolution of the gluconic acid derivative; and

d) recovering the gluconic acid derivative from the purified andconcentrated aqueous solution.

The step of separating the inorganic impurity from the concentratedacidified aqueous solution may be accomplished by several methodsincluding, but not limited to, electrodialysis and anion exchangeresins. This method is particularly favorable when the acidified and/ornon-viable fermentation medium contains a substantial amount of gluconicacid derivative such as KLG in the free acid form.

It is still another object of the present invention to provide processesfor preparing highly purified and concentrated KLG comprising thefollowing steps of

a) providing an acidified and/or non-viable fermentation mediumcomprising at least KLG, an inorganic impurity and a neutral;

b) removing at least the KLG and inorganic impurity from the acidifiedand/or non-viable fermentation medium by electrodialysis therebyproviding a concentrated acidified aqueous solution comprising at leastthe KLG and inorganic impurity, and a waste stream comprising a spentacidified and/or non-viable fermentation medium substantially depletedof KLG; and

c) separating the inorganic impurity from the concentrated acidifiedaqueous solution by electrodialysis thereby providing a purified andconcentrated aqueous solution of KLG.

Recovery of the purified KLG may be accomplished by any recovery methodwell known in the art including evaporative crystallization or directdrying.

Step (b) of the electrodialysis process may be accomplished by a firstelectrodialysis stack comprising:

(i) an anode in an anolyte compartment, the anode in contact with ananolyte stream, a cathode in a cathode compartment, the cathode incontact with a catholyte stream, and an electrodialysis (hereinafter ED)membrane stack disposed between the anode and the cathode. The EDmembrane stack comprises at least one feed compartment, at least oneconcentrate compartment and alternating anion and cation exchangemembranes dispersed between the feed and the concentrate compartments.The anion exchange membranes must preferentially transport KLG anionsand inorganic anions to the exclusion of neutrals in the acidifiedfermentation medium. The acidified and/or non-viable fermentation mediumis introduced into the feed compartment and an aqueous solutioncontaining an acid or salt is introduced into the concentratecompartment. A sufficient voltage is applied across the anode andcathode such that protons or other cations migrate across the cationexchange membrane into the concentrate compartment and KLG anions andinorganic anions are transported across the anion exchange membrane intothe concentrate compartment wherein a concentrated acidified aqueoussolution is collected comprising at least KLG and inorganic impurities.The acidified and/or non-viable fermentation medium is essentiallydepleted of KLG and removed from the system as a waste stream.

Step (c) of the electrodialysis process may be accomplished by a secondelectrodialysis stack comprising:

i) an anode in an anolyte compartment, the anode in contact with ananolyte stream, a cathode in a cathode compartment, the cathode incontact with a catholyte stream, and an ED membrane stack disposedbetween the anode and the cathode. The ED membrane stack comprises atleast one feed compartment, at least one concentrate compartment andalternating anion and cation exchange membranes dispersed between thefeed and the concentrate compartments. The anion exchange membranes mustpreferentially transport inorganic anions and to the exclusion of KLGanions in the concentrated acidified aqueous solution. The concentratedacidified aqueous solution is introduced into the feed compartment and aaqueous solution containing an acid or salt is introduced into theconcentrate compartment. A sufficient voltage is applied across theanode and cathode such that protons or other cations migrate across thecation exchange membrane into the concentrate compartment and inorganicanions are transported across the anion exchange membrane into theconcentrate compartment. The KLG remains in the feed stream therebyproviding a purified and concentrated aqueous solution of KLG.

The acidified and/or non-viable fermentation medium of the presentinvention preferably has a pH of less than 4.5, and more preferably lessthan 3.5, and most preferably less than 2 wherein the gluconic acidderivative and specifically KLG is substantially protonated.Substantially protonated as used herein means the gluconic acidderivative is at least 80% protonated and preferably greater than 90%protonated.

In an alternative embodiment, step (c) for separating the inorganicimpurities may be performed before step (b) in the above process.

In the first electrodialysis stack, KLG and inorganic impurities areremoved from the acidified and/or non-viable fermentation medium whereinKLG anions, as well as inorganic anions if present, are transportedacross an anion exchange membrane. In this instance, the membranerejects the passage of neutrals. Hereinafter, this first electrodialysiscell is referred to as “KLG ED”.

In the second electrodialysis stack, inorganic impurities such as acidsor salts are separated from KLG by using anion exchange membranes whichare permselective for inorganic anions but which do not transport KLGanions. The anion exchange membranes must have a very high resistance toKLG anion transport so that inorganic anions will be transported withminimal loss of KLG. Hereinafter, this second electrodialysis stack isreferred to as “Desalting ED.” Desalting ED refers to the removal ofinorganic acids as well as inorganic salts.

It has been discovered by the inventors that an in-vitro reactorprovides a more efficient and cost effective method for producing KLG ifthe coenzymes used as redox cofactors in the chemical synthesis ofgluconic acid derivatives can be reused by returning the coenzymes tothe in vitro reactor. The advantages of using the in-vitro reactor whichhas no living and metabolically active cells or microorganisms in thein-vitro reactor medium are numerous including the fact that alternativemetabolic pathways used by living cells are shut down. Thus understood,conversion of the substrates, such as carbohydrates and/or intermediatemolecules to a preferred end product is predetermined. Therefore, thesubstrates and/or intermediate molecules are not wasted by beingconverted to unwanted byproducts. Instead, the most effecient pathway ofconversion is used thereby producing higher yields from the substratesor intermediate molecules to the preferred gluconic acid derivative.

Using an in-vitro reactor, the cells, if any, containing oxidizing andreducing enzymes are dead and/or non-existent and conversion to agluconic acid derivative salt is strictly by a chemical redox reaction.However, coenzymes, used as redox cofactors in the chemical synthesis ofgluconic acid derivatives, are needed in the reactor medium and recoveryof these coenzymes is essential because of the high cost of replacement.With this in mind, the inventors have discovered a method usingelectrodialysis to recover these expensive and valuable coenzymes forreuse or recirculation back into the reactor vessel.

Thus understood, it is yet another object of the present invention todisclose processes for preparing highly purified and concentrated KLGcomprising the following steps of:

a) providing an in vitro reactor medium comprising at least a gluconicacid derivative anion, a metal counterion and a coenzyme; and

b) introducing the in vitro reactor medium to an electrodialysis cellcomprising at least one bipolar membrane wherein the gluconic acidderivative anion is protonated and the metal counterion adds a hydroxideion thereby providing at least a concentrated aqueous solutioncomprising a gluconic acid derivative and a stream comprising a metalhydroxide solution. In addition a separate stream comprising thecoenzyme may be included in the process.

Several different bipolar membrane electrodialysis (ED) stacks may beused in this embodiment including a two or three compartment bipolarmembrane electrodialysis stack. The two compartment stack comprises ananode in an anolyte compartment, the anode in contact with an anolytestream, a cathode in a cathode compartment, the cathode in contact witha catholyte stream, and a two compartment bipolar membrane ED stackdisposed between the anode and the cathode. The two compartment bipolarmembrane ED stack comprises at least one anion exchange membrane, abipolar membrane positioned on opposite sides of the anion exchangemembrane and spaced sufficiently to provide at least one feedcompartment and at least one concentrate compartment, the anode andcathode positioned on different ends of the cell connected to a powersource for providing an electric current through the cell stack. Theanion exchange membranes must preferentially transport gluconic acidderivative anions, such as KLG anions, and inorganic anions to theexclusion of neutrally charged molecules. The in-vitro reactor mediumcontaining at least the salt of a gluconic acid derivative is introducedinto the feed compartment. Water or an aqueous solution of a gluconicacid derivative or a salt thereof is introduced into the concentratecompartment. A voltage is applied across the anode and cathodesufficient to dissociate water to form a proton and hydroxide ion at thebipolar membranes and to transport the gluconic acid derivative anionacross the anion exchange membrane into the concentrate compartment ofthe bipolar membrane ED stack. Gluconic acid derivative anions aretransported across the anion exchange membrane while the passage ofneutrals are prevented. The gluconic acid derivative anion is convertedto its acid form once it has been transported into the concentrate oracid compartment by the addition of proton formed at a bipolar membrane.The cation originally associated with the gluconic acid derivative anionin the feed solution is converted to a base by addition of the hydroxideion formed at the bipolar membrane. The net effect is the formation ofconcentrated and purified gluconic acid derivative, such as KLG and abase, for example caustic soda, from the splitting of the KLG Na salt.

In the two compartment configuration, the hydroxide ion which displacesthe KLG anion may be neutralized by the addition of CO₂ into the feedsolution so that the pH in the feed compartment remains in a range wherebase catalyzed decomposition of remaining KLG does not occur. As aresult, the products of the two-compartment configuration are a purifiedand concentrated solution of KLG and a solution comprising at least oneor all of the following including a metal carbonate or bicarbonate, ametal hydroxide, and coenzymes.

The three compartment bipolar membrane ED stack is comprised of a feedor diluent compartment disposed between a base compartment and aconcentrate compartment; the base compartment is separated from the feedcompartment by a cation exchange membrane; and the concentratecompartment separated from the feed compartment by an anion exchangemembrane. These three compartment units are bounded on the ends bybipolar membranes, which supply hydroxide ions to the base compartmentand protons to the concentrate compartment. The three compartmentbipolar membrane ED stack consists of at least one group of these threecompartment units disposed between an anode and a cathode. In thethree-compartment configuration, a hydroxide ion is introduced to thebase compartment where it combines with a cation which migrates acrossthe cation exchange membrane from the feed compartment. Therefore, theaddition of a buffering agent such as CO₂ to the base is not necessarilyneeded because the feed solution of a gluconic acid derivative, such asKLG is isolated from the base by the cation membrane. In thealternative, CO₂ may be included if the preferred end product in thebase solution is a carbonate or bicarbonate. Thus, the products of thethree-compartment configuration are a purified and concentrated solutionof KLG in the concentrate compartment, a solution of metal hydroxidefrom the base compartment and a stream containing at least a coenzymethat may be collected and reused or recirculated back into the reactorvessel. If there are any neutrals included in the feed solution, theyremain therein.

Common to both the two and three compartment configurations is the anionexchange membrane, which must have a low resistance to gluconic acidderivative anion transport and should be selective for gluconic acidderivative anion transport over the transport of any neutrals that maybe found in the feed solution.

A purified solution of a gluconic acid derivative, such as KLG isproduced which is suitable for recovery by further processing viaevaporative crystallization or other recovery techniques, such as directdrying including spray drying or thin film evaporation. If unwantedinorganic acids are removed, a higher recovery of KLG is expectedbecause the potential for acid catalyzed decomposition of KLG uponconcentration is removed. The separation of organic impurities such asneutrals from the KLG allows greater recovery of KLG because anyincreased viscosity that may be due to inclusion of neutrals is reducedduring evaporation. Furthermore, KLG that has been purified by ED may bespray dried without suffering loss of yield during downstream conversionto ascorbic acid.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagrammatic view of the ED membrane cell used forseparating an acidified and/or non-viable fermentation medium comprisingat least a gluconic acid derivative and specifically KLG (KLG ED) fromany neutrals in the medium.

FIG. 2 is a diagrammatic view of the ED membrane cell used forseparating inorganic impurities from an acidified and/or non-viablefermentation medium comprising at least a gluconic acid derivative, suchas KLG (Desalting ED).

FIG. 3 is a diagrammatic view of the two compartment bipolar membrane EDcell used for the concentration and purification of a gluconic acidderivative, such as KLG from a viable or non-viable fermentation medium;or an in-vitro reactor medium(Salt Splitting KLG ED).

FIG. 4 is a diagrammatic view of the three compartment bipolar membraneED cell used for the concentration and purification of a gluconic acidderivative and specifically KLG from a viable or non-viable fermentationmedium (Salt- Splitting KLG ED).

FIG. 5 is a diagrammatic view of the three compartment bipolar membraneED cell used for the concentration and purification of a gluconic acidderivative and specifically KLG from an in-vitro reactor medium (Salt-Splitting KLG ED).

DESCRIPTION OF THE PREFERRED EMBODIMENTS

In one embodiment of the present invention, wherein the feed solution isan acidified and/or non-viable fermentation medium, the gluconic acidderivative and or salt thereof, such as KLG, may be produced by livemicroorganisms metabolizing carbohydrates in a fermentation process. Anymicroorganism capable of converting carbohydrates to a gluconic acidderivative or the salt thereof and specifically 2-keto-L-gulonic acid orsalt thereof may be used in the present invention.

Before concentration and purification of a gluconic acid derivative suchas KLG, the fermentation broth is preferably pretreated by any one orall of the following: (i) filtration or centrifuge to remove anymicrobial cells and other particulates; (ii) acidification by additionof an acid, such as sulfuric acid that serves to protonate the KLG andto precipitate the majority of cations that were introduced into thebroth during the fermentation process (used to maintain an acceptable pHlevel for ensuring viability of the microorganisms) thereby providing anon-viable and/or acidified fermentation medium; (iii) carbon treatmentto adsorb color bodies and other organic impurities; (iv) cationexchange resins, such as Amberlite IRC 120, Amberlite 200C to morecompletely protonate any remaining KLG anions and/or to remove solublecations, such as calcium; (v) anion exchange resins, such as AmberliteIRA 93, Amberlite IRA 94 to remove inorganic or organic impurities whichmay foul the ED membranes; (vi) treatment with polymeric adsorbentresins to remove impurities; and (vii) removal of inorganic acids orsalts such as sulfuric acid by desalting ED (see description of FIG. 2).Also, a stable anion or cation exchange resin or mixtures thereof may beadded to the feed solution compartment to provide enhanced masstransport of the inorganic ions to the membrane surfaces (if included inthe feed solution).

If the solution has already been treated by evaporative crystallizationfor recovery of KLG, then the electrodialysis cell of FIG. 1 may be usedon the crystallization mother liquor to remove neutrals and to allowfurther concentration and recovery of KLG.

The fermentation broth which is acidified and/or essentially non-viableis introduced into an electrodialysis stack such as represented in FIG.1. The KLG ED process and the ED cell stack are used for removing atleast KLG from the acidified and/or non-viable fermentation broth whileleaving neutrals in the non-viable fermentation broth. The components ofthe KLG ED stack include an anode (2) and cathode (4) rinsed with anelectrolyte, and an electrodialysis cell stack (5) comprising at leastone feed compartment (6) and one concentrate compartment (8) disposedbetween the anode and cathode, the at least one feed and concentratecompartment are separated by alternating anion and cation exchangemembranes, (10) and (12) respectively.

The anode (2) should be stable to the electrodialysis conditions and mayinclude carbons such as graphite, noble metals or alloys of Pt, Pd, Ir,Au, Ru, etc., noble metals or alloys deposited on a valve metal such asTi or Ta, etc. Generally, the anode reaction will be the oxidation ofwater to produce oxygen and protons (Equation 1).

2H₂O→O₂+4H⁺+4e ⁻  (1)

The cathode (4) may include carbons, noble metals and alloys, nickel,steels, etc. Generally, the cathode reaction is the production ofhydrogen and hydroxide from the reduction of water according to reaction2.

2H₂O+2e ⁻→H₂+2OH⁻  (2)

The anode and cathode are rinsed with an electrolyte and typically theanolyte and catholyte solutions are a solution of an inert strong acid,base, or salt such as sulfuric acid, sodium hydroxide, or sodiumsulfate.

Introduced into the feed compartment (6) is a feed electrolyte solutioncomprising an acidified and/or a non-viable fermentation mediumcomprising at least a gluconic acid derivative such as KLG.

Introduced into the concentrate compartment (8) shown in FIG. 1 is aconcentrate solution that initially comprises deionized water, or asolution of KLG or salt thereof dissolved in water in a sufficientamount to provide conductivity in the solution.

The KLG ED cell stack diagramed in FIG. 1 is further comprised of atleast one alternating anion (10) and cation (12) exchange membraneseparating the feed and concentrate compartments. The cation exchangemembranes may be of weak acidity (e.g. carboxylic acid type), moderateacidity (e.g. phosphonic acid type), or strongly acidic (sulfonic acidcation exchange groups). The cation membranes must be stable to theelectrodialysis conditions, should have a low resistance in the gluconicacid derivative solution to be dialyzed, and may include perfluorinatedmembranes such as DuPont Nafion® or any non-perfluorinated cationexchange membrane such as Neosepta CMX both of which are commerciallyavailable. The anion exchange membranes may be strongly, mildly, orweakly basic and are typically comprised of quaternary or tertiaryammonium groups. The anion exchange membranes must also be stable in theconditions of the stack and should have a sufficiently open porestructure such that gluconic acid derivative anion transport can occurat reasonably low potentials. Furthermore, the anion exchange membraneshould substantially prevent transport of any neutrals present in thefeed stream. A preferred anion exchange membrane is Neosepta AFX. Aplurality of these two compartment units comprised of anion and cationexchange membranes may be stacked together in an electrodialysis stackwith at least a pair of electrodes at the outer and opposite ends of thecell.

Under the influence of a potential field, the voltage determinant uponthe number of pairs of membranes and preferably ranging from 0.1 to 10volts per pair, the cations will migrate towards the cathode (4) throughthe cation exchange membrane (12) into the concentrate compartment(8).The anion of the gluconic acid derivative, and specifically KLG anions,will migrate towards the anode (2) across the anion exchangemembrane(10) into the concentrate compartment (8) forming a purified andconcentrated solution of KLG in the concentrate and leaving behind theneutrals in the feed solution. In this manner, KLG may be nearlycompletely removed from the feed solution, concentrated by a factor ofup to approximately 3-4 times or more, and separated from any neutrals.As a result of the separation of KLG from neutrals in the feed stream,recovery of KLG by direct drying of the concentrate may be practiced.

Any inorganic anions present such as chloride, sulfate, or phosphatewill be transported preferentially over the transport of a gluconic acidderivative anion into the concentrate. If the inorganic anions arepresent as acids in the concentrate, the buildup of inorganic acids inthe KLG ED concentrate may initiate proton back-migration. Thisback-migration may be prevented by any of the following means: (i)addition of a strong base such as sodium hydroxide to the concentrate inan amount sufficient to neutralize the inorganic acids; (ii) inorganicacids are removed in a first cut of the concentrate which is largelyfree of the gluconic acid derivative because the inorganic acids aretransported preferentially to the gluconic acid derivative; (iii) anionexchange resins for removal of strong acids from the concentrate; and(iv) concurrent operation of a Desalting ED stack to remove inorganicacids from the concentrate nearly as quickly as they build up by feedingthe concentrate from the KLG ED stack to a Desalting ED stack (as shownin FIG. 2). These four techniques all prevent the buildup of strongacids in the concentrate and subsequent proton back-migration across theanion exchange membrane which may cause a loss in current efficiency. Asa further benefit, the acid catalyzed decomposition of a gluconic acidderivative, such as KLG is avoided during evaporative crystallization ordirect drying.

The KLG ED cell stack diagramed in FIG. 1 may be operated at a unit cellvoltage from about 0.1 to about 10 volts per anion/cation exchangemembrane pair and more preferably from about 0.5 to about 3 volts perpair. The temperature range should be between about 5° C. to about 90°C. and more preferably from about 20° C. to about 50° C. Highertemperatures may cause degradation of some of the membranes and of thegluconic acid derivative, and therefore should be avoided. The processmay be run continuously or in a batch mode.

One of the preferred processes for separating inorganic impurities fromthe concentrate solution of a gluconic acid derivative, and specificallyKLG, is shown in FIG. 2. This figure diagrams the Desalting ED processand the membrane configuration in the ED membrane cell stack used forseparating inorganic acids or salts from an acidified and/or non-viablefermentation medium comprising KLG or the concentrate of KLG produced inthe electrodialysis cell shown in FIG. 1. The components of theelectrodialysis stack include an anode (20) and cathode (22) rinsed withan electrolyte, and an electrodialysis cell stack (24) having at leastone feed compartment (26) and one concentrate compartment (28) disposedbetween the anode and cathode wherein the feed and concentratecompartments are separated by alternating anion and cation exchangemembranes, (30) and (32), respectively.

Initially introduced into the concentrate compartment (28) of thedesalting ED stack is either deionized water or a solution of inorganicacid or salt dissolved in water. Introduced into the feed compartment(26) is a feed electrolyte solution which may include; a non-viableand/or acidified fermentation medium; a solution of the preferredgluconic acid derivative and/or the salt of the derivative dissolved inwater; or the concentrate solution obtained from the electrodialysiscell shown in FIG. 1 comprising at least a gluconic acid derivative,such as KLG, and inorganic impurities.

Typically, the feed solution will be derived from a fermentation brothwhich has been rendered acidified and/or non-viable and may comprise anyone or all of the following including debris from non-livingmicroorganisms such as cells, neutrals, alkali cations, and inorganicacids. Pretreatment steps for the feed solution may comprise any one orall of the following: (i) filtration to remove cells and otherparticulates; (ii) acidification by addition of a convenient acid suchas sulfuric acid that serves to protonate the salt of a gluconic acidderivative, such as KLG and to precipitate the majority of cations suchas calcium sulfate (if the KLG was present as the calcium salt prior toacidification) and providing a non-viable and/or acidified fermentationmedium; (iii) carbon treatment to adsorb color bodies and other organicimpurities; (iv) cation exchange to more completely protonate the saltof a gluconic acid derivative and/or to remove soluble calcium; (v)anion exchange to remove impurities which may foul the ED membranes;(vi) treatment with polymeric adsorbent resins to remove impurities;(vii) evaporative crystallization; and (viii) removal of neutrals by theelectrodialysis stack descnbed in FIG. 1. Also, a stable anion or cationexchange resin or mixtures thereof may be added to the feed electrolytesolution compartment to provide enhanced mass transport of the inorganicions to the membrane surfaces.

The desalting ED cell stack is further comprised of at least onealternating anion (30) and cation (32) exchange membrane separating thefeed and concentrate compartments. The cation exchange membranes may beof weak acidity (carboxylic acid exchange groups), moderate acidity(e.g. phosphonic acid type), or strongly acidic (e.g. sulfonic acidcation exchange groups). The cation exchange membranes must be stable tothe conditions used in electrodialysis cell, should have a lowresistance in the solution to be dialyzed, and may includeperfluorinated membranes such as DuPont Nafion® or anynon-perfluorinated cation exchange membrane such as Neosepta CMX. Theanion exchange membranes may be strongly, mildly, or weakly basic andcomprised of quaternary or tertiary ammonium groups. The anion exchangemembranes must also be stable and should have a sufficiently tight porestructure such that inorganic anions such as chloride or sulfate willtransport through the membrane while transport of a gluconic acidderivative anion is substantially or entirely prevented. Furthermore, ifremoval of inorganic acids is desired, the anion exchange membraneshould preferably be a low proton back-migration type such as AsahiGlass Selemion AAV or Neosepta ACM. This type of membrane will improvethe current efficiency of the process by preventing back-migration ofprotons from the concentrate compartment to the feed compartment.

Alternatively, the inorganic acids in the concentrate compartment may beneutralized with a strong base such as sodium hydroxide so that protonback-migration is prevented.

Many of these two compartment units comprised of anion and cationmembranes may be stacked together in an electrodialysis stack with atleast a pair of electrodes at the outer ends.

Under the influence of a potential field, cations will migrate towardsthe cathode (22) through the cation exchange membrane (32)into theconcentrate compartment (28). Inorganic anions will migrate towards theanode (20)across the anion exchange membrane (30)into the concentratecompartment (28) forming a solution of inorganic acid or salt andleaving behind a purified solution of a gluconic acid derivative in thefeed solution (if the original feed solution is the concentrate from theelectrodialysis stack described in FIG. 1). When the inorganic anionsare depleted, the cell current will drop to nearly zero because thegluconic acid derivative anions that remain in the feed aresubstantially prevented from transporting through the anion exchangemembrane by the structure of the membrane.

The Desalting ED cell stack diagramed in FIG. 2 may be operated at aunit cell voltage from about 0.1 to about 10 volts per anion/cationexchange membrane pair and more preferably from about 0.5 to about 3volts per pair. The temperature range should be between about 5° C. toabout 90° C. and more preferably from about 20° C. to about 50° C.Higher operating temperatures may cause degradation of the membranes andof the gluconic acid derivative. The process may be run continuously orin a batch mode.

FIGS. 3, 4 and 5 diagram the Salt-splitting KLG ED processes and the twoor three compartment bipolar membrane ED cell stacks used therein. Inthe Salt-splitting KLG ED process, a salt of a gluconic acid derivative,such as KLG is converted to purified and concentrated KLG.

The components of the two compartment electrodialysis stack shown inFIG. 3 include an anode (40) and cathode (42) rinsed with anelectrolyte, and an electrodialysis cell stack (43) having at least onefeed compartment (44) and one concentrate compartment (46) disposedbetween the anode and cathode. The feed and concentrate compartments areseparated by an anion exchange membrane (48). A bipolar membrane (50) ispositioned on both sides of the anion exchange membrane.

Introduced into the feed compartment (44) of the two compartment bipolarmembrane ED cell stack is a feed electrolyte solution which may includean in-vitro reactor medium comprising at least the salt of a gluconicacid derivative and coenzymes; a non-viable fermentation mediumcomprising at least a salt of a gluconic acid derivative; a solutioncontaining a salt of the derivative; or a KLG salt dissolved in water.The salt of the derivative should be chosen so that it does not forminsoluble precipitates upon the addition of base, otherwise, theseprecipitates could foul the bipolar membrane or cation membranes.Representative examples of suitable salts include alkali metal saltssuch as sodium and potassium, or ammonium salts.

If the feed is derived from a viable or non-viable fermentation medium,pretreatment steps for the solution shall include any one or all of thepretreatment steps discussed above including:(i) filtration to removecells and other particulates; (ii) carbon treatment to adsorb colorbodies and other organic impurities; (iii) addition of an inorganic acidsuch as sulfuric acid to protonate the salt of the gluconic acidderivative and precipitate the metal counterion as a sulfate renderingthe fermentation medium acidified and/or non-viable(iv) addition of analkali metal salt such as sodium sulfate or sodium carbonate that willprecipitate calcium as the sulfate or carbonate and form an alkali metalsalt of the gluconic acid derivative which is suitable for saltsplitting ED in a bipolar membrane ED stack; (v) cation exchange toremove divalent metals that would otherwise form membrane-foulingprecipitates upon contact with base; (vi) anion exchange to removeimpurities which may foul the ED membranes; (vii) treatment withpolymeric adsorbent resins to remove impurities; and (viii) removal ofinorganic salts such as sodium sulfate by desalting ED (see descriptionof FIG. 1).

Also, a stable anion or cation exchange resin or mixtures thereof may beadded to the feed solution compartment to provide enhanced masstransport of the inorganic ions to the membrane surfaces.

Introduced into the concentrate compartment (46) of the two compartmentbipolar membrane ED cell stack is a concentrate solution that can becomprised initially of deionized water or of a solution of a gluconicacid derivative which is being concentrated, such as KLG dissolved inwater.

The two compartment bipolar membrane electrodialysis cell stack of FIG.3 is further comprised of an anion exchange membrane (48) and at leastone bipolar membrane (50), wherein the anion exchange membrane separatesthe feed and concentrate compartments. The bipolar membrane consists ofan anion exchange layer bonded to a cation exchange layer, such asNeosepta BP-1 or others. This membrane dissociates water to form ahydroxide ion and a proton at a low potential. The anion exchangemembrane may be strongly, mildly, or weakly basic and comprised ofquaternary or tertiary ammonium groups. The anion exchange membranesmust be stable to the conditions within the electrodialysis cell andshould have a sufficiently open pore structure such that gluconic acidderivative anion transport can occur at reasonably low potentials.Furthermore, the anion exchange membrane should prevent transport of anyneutrals. Many of these two compartment units comprised of anion andbipolar membranes may be stacked together in an electrodialysis stackwith at least one pair of electrodes at the outer ends.

Under the influence of a potential field, water will be dissociated inthe bipolar membrane to form hydroxide ions and protons. Hydroxide ionswill migrate towards the anode (40) into the feed compartment (44) ofthe two compartment bipolar membrane ED cell where they will combinewith a metal cation, such as Na⁺, to form a base such as sodiumhydroxide. Carbon dioxide, which may be available because it is abyproduct of the fermentation process, may also be added to the feed toneutralize the hydroxide so that the feed pH does not become so alkalinethat the gluconic acid derivative is decomposed. Protons will movetowards the cathode (42) into the concentrate compartment (46) wherethey will combine with gluconic acid derivative anions which migratetowards the anode (40) across the anion membrane (48), thereby forming apurified and concentrated solution of a gluconic acid derivative andleaving behind, in the feed solution, any neutrals and/or coenzymes. Thecomposition of the remaining feed solution is dependent upon the initialtype of medium such as an in-vitro reactor medium or an acidified and/ornon-viable fermentation medium. A gluconic acid derivative, such as KLGmay be nearly completely removed from the feed solution, concentrated byup to a factor of approximately 3-4 times or more. As a result of thepurification of KLG subsequent recovery of KLG may be accomplished bydirect spray drying of the concentrate.

The three compartment bipolar membrane ED stack (58) shown in FIGS. 4and 5 consist of at least three compartment units disposed between ananode (66) and a cathode (68). The three compartment bipolar membrane EDstack comprises a feed or diluent compartment (60) disposed between abase compartment (64) and a concentrate compartment (62); the basecompartment is separated from the feed compartment by a cation exchangemembrane (70), and the concentrate compartment (62) is separated fromthe feed compartment (60) by an anion exchange membrane (72). Thesethree compartment units are bounded on the ends by bipolar membranes(74), which are bathed in an anolyte and catholyte rinse stream andthereby supplying hydroxide ions to the base compartment (64) andprotons to the concentrate compartment(62). The bipolar and anionmembranes are further described in the description of the twocompartment bipolar membrane ED cell stack above. The cation exchangemembranes may be of weak acidity (e.g. carboxylic acid type), moderateacidity (e.g. phosphonic acid type), or strongly acidic (sulfonic acidcation exchange groups). The cation exchange membranes must be stable inthe conditions of the bipolar membrane ED stack, should have a lowresistance in the gluconic acid derivative solution to be dialyzed, andmay include perfluorinated membranes such as DuPont Nafion® or anynon-perfluorinated cation exchange membrane such as Neosepta CMX. Manyof these three compartment units comprised of bipolar, cation exchange,and anion exchange membranes may be stacked together in anelectrodialysis stack with at least one pair of electrodes at the outerends.

Under the influence of a potential field, water will be dissociated inthe bipolar membranes (74) to form hydroxide ions and protons. Ahydroxide ion will migrate towards the anode (66) into the basecompartment (64) of the three compartment bipolar membrane ED cell whereit will combine with a metal cation which is transported from the feedcompartment (60) across the cation exchange membrane (70) to form a basesuch as sodium hydroxide. Protons will move towards the cathode (68)into the concentrate compartment (62) where they will combine withgluconic acid derivative anions which migrate towards the anode (66)across the anion exchange membrane (72), thereby forming a purified andconcentrated solution of a gluconic acid derivative, such as KLG andleaving behind any neutrals in the feed solution such as shown in FIG. 4if the feed solution is an acidified and/or non-viable fermentationmedium.

Introduced into the feed compartment (60) of the three compartmentbipolar membrane ED cell stack is a feed electrolyte solution which mayinclude an in-vitro reactor medium comprising at least the salt of agluconic acid derivative and coenzymes; a non-viable fermentation mediumcomprising at least a salt of a gluconic acid derivative; a solutioncontaining a salt of the derivative; or a KLG salt dissolved in water.The salt of the derivative should be chosen so that it does not forminsoluble precipitates upon the addition of base, otherwise, theseprecipitates could foul the bipolar membrane or cation membranes.Representative examples of suitable salts include alkali metal saltssuch as sodium and potassium, or ammonium salts.

Introduced into the concentrate compartment (62) of the threecompartment bipolar membrane ED cell stack is a concentrate solutionthat can be comprised initially of deionized water or of a solution of agluconic acid derivative which is being concentrated, such as KLGdissolved in water. Deionized water and/or a basic aqueous solutioncomprising NaOH or KOH may be introduced into the base compartment (64).

In a preferred embodiment shown in FIG. 5, the feed solution comprisesan in-vitro reactor medium comprising at least a salt of a gluconic acidderivative and a coenzyme wherein the valuable coenzymes remain in thefeed solution and can be drawn off for reuse or recirculated into thein-vitro reactor. KLG may be nearly completely removed from the feedsolution, concentrated by up to a factor of approximately 3-4 times ormore.

In both the two and three compartment bipolar membrane ED stacks, if anyinorganic anions are present in the feed solution they may betransported into the concentrate compartment preferentially to gluconicacid derivative anions. The inorganic anions may combine with protonsformed at the bipolar membranes which will result in the buildup ofinorganic acids in the concentrate and cause proton back-migration witha concomitant loss of current efficiency. This may be prevented by anyof the following means: (i) addition of a strong base such as sodiumhydroxide to the concentrate in an amount sufficient to neutralize theinorganic acids; (ii) the inorganic acids are removed in a first cut ofthe concentrate which is largely free of any gluconic acid derivativesbecause the inorganic acids are transported preferentially to gluconicacid derivatives; (iii) concurrent operation of a Desalting ED stack toremove inorganic acids from the concentrate nearly as quickly as theybuild up by feeding the concentrate from the Salt-splitting KLG ED stackto a Desalting ED stack; and (iv) anion exchange for removal of strongacids from the concentrate. These four techniques all prevent thebuildup of strong acids in the concentrate and possible protonback-migration across the anion exchange membrane. As a further benefit,the acid catalyzed decomposition of gluconic acid derivatives andspecifically KLG is avoided during evaporative crystallization or spraydrying.

Also, a stable anion or cation exchange resin or mixtures thereof may beadded to the feed solution compartment to provide enhanced masstransport of the inorganic ions to the membrane surfaces(if contained inthe feed solution).

The Salt-splitting ED cell stacks diagramed in FIGS. 3, 4 and 5 may beoperated at a unit cell voltage from about 0.1 to about 10 volts per setof membranes and more preferably from about 0.5 to about 5 volts perset. The temperature range should be between about 5° C. to about 90° C.and more preferably from about 20° C. to about 50° C. Highertemperatures may cause degradation of some of the membranes and the acidof the gluconic acid derivatives. The process may be run continuously orin a batch mode.

In each of the above embodiments it is possible that impurities in thefeed solution may foul the membranes resulting in loss of performance.The membranes may be cleaned in place (in the ED stack) with varioussolutions including: (i) NaCI solutions; (ii) sodium chloride solutionsat pH 12; (iii) a nitric or other mineral acid solution; and (iv)solutions i, ii, or iii with a non-ionic or ionic detergent added. Otherwash solutions are possible so long as they effect the necessarymembrane cleaning and do not degrade the membrane performance. The cleanin place (CIP) procedure may include an elevated temperature of the washsolution so long as the membranes are stable to the temperatures. TheCIP procedure may also include passage of current through the EDmembrane stack or current reversal; however, bipolar membrane stacksgenerally cannot be subjected to current reversal as this would damagethe bipolar membranes.

The invention will be more clearly perceived and better understood fromthe following examples.

EXAMPLE 1 Removal of Inorganic Acids from KLG Fermentation Broth

In an example of Desalting ED, sulfuric, hydrochloric, and phosphoricacids were removed from a non-viable and acidified fermentation brothcontaining KLG using the electrodialysis stack described in FIG. 2. TheKLG was originally present as the calcium salt in the broth. The brothwas microfiltered to remove the cells, and sulfuric acid was added toprotonate the KLG salt and to precipitate calcium cation as the sulfate.The acidified broth was then cation exchanged to completely removecalcium. The electrodialysis cell used was an Electrosynthesis CompanyED-1 BP cell fitted with a platinized titanium anode and cathode,Selemion AAV low proton back-migration anion exchange membranes (AsahiGlass), and Neosepta CMX (Tokuyama) cation exchange membranes. The areaof the membranes was 100 cm² each (5 pairs), and the inter-membrane gapwas 0.75 mm. The rinse solution was 0.2 molar sulfuric acid. The initialacid compartment solution was 350 ml of water.

The initial feed solution was comprised of 910 ml of an acidified andnon-viable fermentation broth containing 91 gl⁻¹ KLG, 153 ppm chloride,257 ppm phosphate, and 5176 ppm sulfate, all present as the acids. Theexperiment was operated at a controlled cell voltage of 1.6 volts permembrane pair (11 V total cell voltage, assuming combined electrodepotentials of 3 V), and a temperature of 30° C. The final feed containedless than 10 ppm chloride, 34 ppm sulfate, and 120 ppm phosphate. Thetotal charge passed was 2790 coulombs, and the current efficiency was76% for salts removed. The current density range for the experiment wasfrom about 13.5 to about 1.5 mA cm⁻², with the average current densitybeing 6.5 mA cm⁻². Only 1.2% of the KLG present in the feed was lost bytransport into the acid compartment.

EXAMPLE 2 Concentration and Purification of KLG from Fermentation Broth

In an example of the KLG ED process, KLG was concentrated and purifiedin an electrodialysis stack similar to that described above in FIG. 1.The anion exchange membranes chosen were Neosepta AFX, which is amembrane that will transport the KLG anion. The feed solution that beinga non-viable and acidified fermentation medium was pretreated asfollows: A fermentation broth was microfiltered to remove cells, andsulfuric acid was added to protonate the KLG salt and to precipitate thecation calcium as the sulfate. Residual calcium was then removed bycation exchange.

A total of 10 membrane pairs were used giving a membrane area of 1000cm². The anolyte and catholyte were a solution of 0.2 molar sulfuricacid. The initial concentrate consisted of 300 ml of concentrate from aprevious KLG electrodialysis experiment. The initial feed solutionconsisted of 3.5 L of acidified and non-viable fermentation brothcontaining 142.4 g l⁻¹ KLG. The inorganic ion concentrations were: 241mg l⁻¹ Cl⁻, 565 mg l⁻¹ PO₄ ³ ⁻, and 1277 mg l⁻¹ SO₄ ²⁻. The feed waspretreated as described above. The experiment was operated at acontrolled cell voltage of 2.7 volts per membrane pair or 30 volts totalcell voltage, and a temperature of 45° C. The inorganic acids whichtransported into the concentrate were neutralized with 50% NaOH toprevent proton back-migration. After 213 minutes, 95.1% of the KLG wasremoved from the feed and transported into the concentrate, giving afinal KLG concentration of 435.4 g l⁻¹ in the concentrate. The currentdensity range was from about 70.0 to about 8.4 mA cm⁻², with the averagebeing 26.8 mA cm⁻². The current efficiency was 67% for KLG transport.The KLG was concentrated approximately three times by ED.

Table 1 shows sugar analyses from a typical ED run where KLG isconcentrated and purified using the AFX anion exchange membrane. 95% ofthe KLG was transported into the concentrate, but the table shows thatmost of the sugars were retained in the feed.

TABLE 1 Retention of Sugars During AFX ED of KLG Broth Initial Feedconcentration, Final Feed % Retention g/L concentration, g/L RetainedComponent Time, min (total amt, g) (total amt, g) in Feed Maltose 10.7 6.84 (23.94)  8.97 (23.55) 98 Glucose 12.3 1.97 (6.90) 2.29 (6.01) 87Fructose 13.4 1.61 (5.64) 1.73 (4.54) 80 General ED Conditions: 3.5 L offermentation broth electrodialyzed at 2.7 volts/pr. membranes in a 10pr. ED stack. Broth pretreated by sulfuric acid addition to precipitatecalcium sulfate, followed by cation exchange; 95% of the KLGtransported.

Table 2 shows the improved recovery of KLG and yield of ascorbic acid(AsA) afforded by ED. The table shows that ED coupled with direct dryinggives a better overall yield to ascorbic acid than any other recoverymethod. Conventional crystallization (Process B), when pushed to higherrecovery of KLG (90%) by the use of multiple crop crystallization, givesa poor yield from KLG to AsA and therefore a lower overall yield. Thisoccurs because the presence of neutrals in the broth results inviscosity buildup during multiple crop crystallization, and as a result,poor separation of neutrals from KLG in the crystallization step. Theneutrals are then carried into the AsA conversion process where theycause poor yields. Direct drying of the fermentation broth without ED(Process C) suffers the same problem; neutrals in the broth contaminatethe KLG and as a result yields to AsA and overall process yields arelow.

TABLE 2 Improvement of KLG Recovery and AsA Yield with ED Step YieldsRecov- AX/ Con- ery Anion Process version Overall Process CX ED A, B, Cto AsA Impurity Profile Yield A 0.98 0.99 0.95 0.866 <1% Inorg. salts0.80 15% organic acids 1% neutrals B 0.98 0.99 0.86 0.907 3% Inorg.salts 0.76 0.5% organic acids 0.5% neutrals 0.98 0.99 0.90 0.830 1%Inorg. salts 0.72 1% organic acids 8% neutrals C 0.98 0.99 1.00 0.774<1% Inorg. salts 0.75 1% organic acids 16% neutrals Recovery Process A =Microfilter, acidify with sulfuric acid, cation exchange, Selemion AAVED for inorganic anion removal, Neosepta AFX ED forconcentration/purification of KLG at 95% recovery, direct drying ofconcentrate. Recovery Process B = Microfilter, acidify with sulfuricacid, cation exchange, anion exchange, crystallize. Recovery Process C =Microfilter, acidify with sulfuric acid, cation exchange, anionexchange, direct drying of broth.

ED alleviates these problems by separating the neutrals from the KLG. EDof the inorganic anions can also be used to replace anion exchange.Direct drying of the ED concentrate gives a high yield of KLG product,which is substantially free of neutrals. As a result, yield conversionsto AsA are good and the overall process yields and economics aresuperior to the other recovery techniques. Furthermore, ED allows theuse of spray drying instead of crystallization, which results inconsiderable capital cost savings.

EXAMPLE 3 Salt-Splitting KLG ED in a Three Compartment Bipolar MembraneCell Stack

A potassium salt of KLG is removed from an in-vitro reactor andintroduced into a three compartment bipolar membrane cell stackdescribed in FIG. 5. The feed solution to the electrodialysis cell is anin-vitro reactor medium comprising 815 ml. of solution containing 121.7grams per liter potassium KLG salt and 0.5 millimolar nicotine adeninedinucleotide phosphate (NADP). The electrodialysis cell is aElectrosynthesis Company ED-1 BP cell fitted with a platinized titaniumanode and cathode, Neosepta BP-1 bipolar membranes, Neosepta AMX-SBanion exchange membranes, and Neosepta CMB (Tokuyama Soda) cationexchange membranes. The area of the membranes is 100 cm² each (4 sets),and the inter-membrane gap is 0.75 mm. The rinse solution was 0.2 molarpotassium sulfate. The concentrate and base compartments were eachfilled with 200 ml of water initially.

The experiment was operated at a controlled cell voltage of 3.25 voltsper set of membranes or 16 volts total cell voltage, and a temperaturefrom about 30° to about 40° C. Above 95% of KLG is removed from the feedand transported into the concentrate where it was converted to the acidform, giving a final KLG acid. Only 1.5% of the coenzyme NADP istransported into the concentrate with the remainder in the feedsolution. The current density range is from about 30.0 to about 4.6 mAcm⁻², with the average being 23.9 mA cm⁻². The current efficiency forKLG formation is 72%.

We claim:
 1. A process for preparing a purified and concentratedgluconic acid derivative comprising the steps of; a) providing anin-vitro reactor medium comprising at least a gluconic acid derivativeanion selected from the group consisting of 2,4, keto-D-gluconic acid,2,5, diketo-D-gluconic acid, idonic acid, 2-keto-L-gluconic acid (KLG),vanillic acid and ascorbic acid, a metal counterion and a coenzyme; andb) introducing the in-vitro reactor medium to an electrodialysis cellcomprising at least one alternating anion and cation exchange membranespaced sufficiently to provide therebetween at least one feedcompartment, a bipolar membrane spaced sufficiently from the cationexchange membrane to provide at least one base compartment therebetween,a bipolar membrane spaced sufficiently from the anion exchange membraneto provide at least one concentrate compartment therebetween, an anodeand cathode positioned on different ends of the cell connected to apower source for providing an electric current through the cell whereinthe gluconic acid derivative anion is protonated and the metalcounterion adds a hydroxide ion to provide at least a concentratedaqueous solution comprising the gluconic acid derivative, a streamcomprising at least a metal hydroxide solution and a waste streamcontaining neutrals.
 2. The process according to claim 1 furthercomprising the step of introducing carbon dioxide to the feedcompartment comprising a metal hydroxide to form a carbonate product insolution selected from the group consisting of a metal carbonate andmetal bicarbonate.
 3. The process according to claim 1 furthercomprising a stream comprising the coenzyme.
 4. The process according toclaim 1 further comprising the step of recovering the gluconic acidderivative from the concentrated aqueous solution.
 5. A process forpreparing a purified and concentrated glulconic acid derivativecomprising the steps of: a) providing a fermentation solution comprisingat least a salt of a gluconic acid derivative selected from the groupconsisting of 2,4, keto-D-gluconic acid, 2,5, diketo-D-gluconic acid,idonic acid, 2-keto-L-gulonic acid (KLG), vanillic acid and ascorbicacid, a metal counterion and a coenzyme; and b) introducing thefermentation solution to an electrodialysis cell comprising at least onealternating anion and cation exchange membrane spaced sufficiently toprovide therebetween at least one feed compartment, a bipolar membranespaced sufficiently from the cation exchange membrane to provide atleast one base compartment therebetween, a bipolar membrane spacedsufficiently from the anion exchange membrane to provide at least oneconcentrate compartment therebetween, an anode and cathode positioned onopposing ends of the cell connected to a power source for providing anelectric current through the cell wherein the gluconic acid derivativeanion is protonated and the metal counterion adds a hydroxide ion toprovide at least a concentrated aqueous solution comprising the gluconicacid derivative, a stream comprising at least a metal hydroxidesolution, and a waste stream containing unionized neutrals.